Enalapril

Enalapril

SCHEMBL6155137

CCOC(=O)C(CCc1ccccc1)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)O.O=C(O)/C=C\C(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACE

The experimentally established mechanism targets of Enalapril. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
ACE known ✓ P12821 14/20 0.91
SMN1; SMN2 Q16637 1/20 1.00
LMNA P02545 2/20 0.91
ABCB11 O95342 2/20 0.65
MEN1 O00255 2/20 0.63
KMT2A Q03164 2/20 0.63
USP2 O75604 1/20 0.63
CYP3A4 P08684 1/20 0.63
ALOX15 P16050 1/20 0.63
PDE3A Q14432 1/20 0.59

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Enalapril SCHEMBL20817249 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL10 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL2719411 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL9 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL10390115 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL1650291 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL308603 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL825430 1.00 SMN1; SMN2 (1.00) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL9019924 0.99 SMN1; SMN2 (0.98) SMN1; SMN2ACELMNAABCB11MEN1
Enalapril SCHEMBL9019927 0.99 SMN1; SMN2 (0.98) SMN1; SMN2ACELMNAABCB11MEN1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 105 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0967221-B1 PROCESS FOR PREPARING PHARMACOLOGICALLY ACCEPTABLE SALTS OF N-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-L-ALANYL AMINO ACIDS KANEKA CORP (JP) 2005-05-25 EP claimed
US-6713628-B2 BY-PRODUCT INHIBITION OF THE DIKETOPIPERAZINE DERIVATIVE BY CARRYING OUT IN AQUEOUS LIQUID A SERIES OF OPERATIONS UNDER GIVEN CONDITIONS IN THE SAME SOLVENT; MAKING ENALAPRIL MALEATE FOR EXAMPLE KANEKA CORPORATION (JP) 2004-03-30 US claimed
US-20030105327-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid KANEKA CORPORATION (JP) 2003-06-05 US claimed
US-6541635-B1 Silylprotected L-proline derivative or salt is deprotected in presence of a nonaqueous medium containing an organic solvent at a temperature of 5 degree C. to 40 degree C. EVERLIGHT USA, INC. 2003-04-01 US claimed
US-20020087007-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid KANEKA CORPORATION (JP) 2002-07-04 US claimed
EP-0967221-A1 PROCESS FOR PREPARING PHARMACOLOGICALLY ACCEPTABLE SALTS OF N-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-L-ALANYL AMINO ACIDS KANEKA CORPORATION (JP) 1999-12-29 EP claimed
US-5977380-A Process for preparing N-[1- (S)-ethoxycarbonyl-3- phenylpropyl]-L-alanine derivatives EVERLIGHT USA, INC. (US) 1999-11-02 US claimed
EP-0463636-A2 Cardiovascular composition MERCK FROSST CANADA INC. (CA) 1992-01-02 EP claimed
US-5001113-A Di- or tripeptide renin inhibitors containing lactam conformational restriction in ACHPA MERCK & CO., INC. (US) 1991-03-19 US claimed
EP-0389127-A1 Renin-inhibitory di-, tri-, and tetrapeptides MERCK & CO. INC. (US) 1990-09-26 EP claimed
US-4782043-A HYPOTENSIVES MERCK & CO., INC. (US) 1988-11-01 US claimed
EP-0278158-A2 Renin inhibitors containing phenylalanyl-histidine replacements MERCK & CO. INC. (US) 1988-08-17 EP claimed
EP-0209897-A2 Peptide enzyme inhibitors MERCK & CO. INC. (US) 1987-01-28 EP claimed
EP-0166257-A2 Cardiovascular composition MERCK FROSST CANADA INC. (CA) 1986-01-02 EP claimed
EP-0163237-A2 Di- and tri-peptidal renin inhibitors MERCK & CO. INC. (US) 1985-12-04 EP claimed
EP-0156318-A2 C-terminal amide cyclic renin inhibitors containing peptide isosteres MERCK & CO. INC. (US) 1985-10-02 EP claimed
EP-0156322-A2 Renin inhibitors containing peptide isosteres MERCK & CO. INC. (US) 1985-10-02 EP claimed
EP-0129189-A2 Renin inhibitors containing a C-terminal amide cycle and compositions and combinations containing the same MERCK & CO. INC. (US) 1984-12-27 EP claimed
US-4472384-A INTERPHENYLENE 9-THIA-11-OXO-12-AZA PROSTANOIC ACID DERIVATIVE AND CARBOXYALKYLDIPEPTIDE MERCK & CO., INC. (US) 1984-09-18 US claimed
US-4374829-A Aminoacid derivatives as antihypertensives MERCK & CO., INC. (US) 1983-02-22 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20030105327-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid SLC7A1, ASS1, ALDH7A1 ACE 67/4885SMN1; SMN2 496/4885LMNA 765/4885
US-20020087007-A1 Process for preparing pharmacologically acceptable salt of N-(1(S)-ethoxycarbonyl-3-phenylpropyl)-L-alanyl-amino acid SLC7A1, ASS1, ALDH7A1 ACE 67/4885SMN1; SMN2 496/4885LMNA 765/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.